As new clinical studies are designed and managed, each study should begin in a well-organized, well-planned manner. This online course assists the clinical study site in preparation for a new clinical study. Topics include identifying the research team, roles and responsibilities of the study coordinator vs. investigators, preparing for a prestudy site visit, review of study protocol, preparing the IRB application, setting up study files and the regulatory binder, and site initiation.
Note: Elective for Professional Certificate in Clinical Trials Design and Management.
Course Number: FPM-40179
Credit: 2.00 unit(s)
Related Certificate Programs: Clinical Trials Design and Management
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4/6/2020 - 6/12/2020
6/22/2020 - 9/5/2020